| Primary Device ID | 04052199273662 |
| NIH Device Record Key | 33aded43-0fae-4f4f-bf07-bffd9cd1c24e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HydroTac transp. comf. 10x20cm st P10 |
| Version Model Number | 685927 |
| Company DUNS | 315768788 |
| Company Name | PAUL HARTMANN AG |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04052199273648 [Primary] |
| GS1 | 04052199273655 [Package] Contains: 04052199273648 Package: [10 Units] In Commercial Distribution |
| GS1 | 04052199273662 [Package] Contains: 04052199273655 Package: [4 Units] In Commercial Distribution |
| NAD | Dressing, Wound, Occlusive |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-09 |
| Device Publish Date | 2020-09-01 |
| 04052199273662 | HydroTac transp. comf. 10x20cm st P10 |
| 04049500835107 | HydroTac transp. comf. 10x20cm st P10 |